The device is intended to be used for in the calibration of Cystatin C assays.

The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values and it is suitable for use on automated analysers.

The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values, and it is suitable for use on automated analysers.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays.

The Randox Liquid Immunoassay Premium - Tri-Level are liquid controls developed for use in the quality control of quantitative assays statedin this package insert.

This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system.

For the quantitative in vitro determination of Total Protein in serum and plasma.

For the quantitative in vitro determination of Total Protein in serum and plasma.

For the quantitative in vitro determination of Total Protein in serum.

This product is intended for in vitro diagnostic use, in the quality control of urine test strips.

This product is intended for in vitro diagnostic use, in the quality control of urine test strips.

The Randox Liquid Urine Control Level 2 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy.

The Randox Liquid Urine Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy.

For the quantitative in vitro determination of total protein in urine and C.S.F.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

The BUN method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of urea nitrogen in serum, plasma and urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.

This product should be used in conjunction with RX SERIES reagents to clean probes and cuvettes.